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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Public Health Genomics Branch
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Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 07, 2024
. (Total: 63788 Documents since 2012)
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ChatGPT accurately performs genetic counseling for gynecologic cancers.
Jharna M Patel et al. Gynecol Oncol 2024 183115-119
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Endometrioid Endometrial RNA Index Predicts Recurrence in Stage I Patients.
Corrine A Nief et al. Clin Cancer Res 2024
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Ethical use of artificial intelligence to prevent sudden cardiac death: an interview study of patient perspectives.
Menno T Maris et al. BMC Med Ethics 2024 25(1) 42
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An AI-based approach driven by genotypes and phenotypes to uplift the diagnostic yield of genetic diseases.
S Zucca et al. Hum Genet 2024
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Population Screening for Hereditary Hemochromatosis
Video Webinar, UNC Precision Public Health Network,
Training Institute for Dissemination and Implementation Research in Genomics and Precision Public Health (TIDR-GPPH)
UNC Precision Public Health Network, March 2024
Recognition of Genetic Conditions After Learning With Images Created Using Generative Artificial Intelligence.
Rebekah L Waikel et al. JAMA Netw Open 2024 7(3) e242609
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A gut microbial signature for combination immune checkpoint blockade across cancer types.
Ashray Gunjur et al. Nat Med 2024
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The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young.
Megan J Puckelwartz et al. Genome Med 2024 16(1) 13
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Unsupervised machine learning to investigate trajectory patterns of COVID-19 symptoms and physical activity measured via the MyHeart Counts App and smart devices.
Varsha Gupta et al. NPJ Digit Med 2023 6(1) 239
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The ENGAGE study: evaluation of a conversational virtual agent that provides tailored pre-test genetic education to cancer patients.
Kala Visvanathan et al. J Cancer Surviv 2023
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The transition from genomics to phenomics in personalized population health.
James T Yurkovich et al. Nat Rev Genet 2023
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Organ aging signatures in the plasma proteome track health and disease.
Hamilton Se-Hwee Oh et al. Nature 2023 624(7990) 164-172
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Enabling the clinical application of artificial intelligence in genomics: a perspective of the AMIA Genomics and Translational Bioinformatics Workgroup.
Nephi A Walton et al. J Am Med Inform Assoc 2023
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The Impact of Artificial Intelligence on Optimizing Diagnosis and Treatment Plans for Rare Genetic Disorders.
Shenouda Abdallah et al. Cureus 2023 15(10) e46860
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Chatbot Artificial Intelligence for Genetic Cancer Risk Assessment and Counseling: A Systematic Review and Meta-Analysis.
Emily M Webster et al. JCO Clin Cancer Inform 2023 7e2300123
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Robust airway microbiome signatures in acute respiratory failure and hospital-acquired pneumonia.
Emmanuel Montassier et al. Nat Med 2023
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Computational immunogenomic approaches to predict response to cancer immunotherapies.
Venkateswar Addala et al. Nat Rev Clin Oncol 2023
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Generation and validation of a classification model to diagnose familial hypercholesterolaemia in adults.
João Albuquerque et al. Atherosclerosis 2023 383117314
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Augmented intelligence facilitates concept mapping across different electronic health records.
Tariq A Dam et al. Int J Med Inform 2023 179105233
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Distinguishing features of Long COVID identified through immune profiling.
Jon Klein et al. Nature 2023
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A machine learning classifier using 33 host immune response mRNAs accurately distinguishes viral and non-viral acute respiratory illnesses in nasal swab samples.
Rushika Pandya et al. Genome Med 2023 15(1) 64
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Machine learning for genetics-based classification and treatment response prediction in cancer of unknown primary.
Intae Moon et al. Nat Med 2023
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The Minimum Data Set for Rare Diseases: Systematic Review.
Filipe Andrade Bernardi et al. J Med Internet Res 2023 25e44641
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Performance of a Cell-Free DNA-Based Multi-cancer Detection Test in Individuals Presenting With Symptoms Suspicious for Cancers.
Alan H Bryce et al. JCO Precis Oncol 2023 7e2200679
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Utilising the precision nutrition toolkit in the path towards precision medicine.
Caleigh Sawicki et al. Proc Nutr Soc 2023 1-11
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Multiple Germline Events Contribute to Cancer Development in Patients with Li-Fraumeni Syndrome.
Vallijah Subasri et al. Cancer Res Commun 2023 3(5) 738-754
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The diagnostic value of electrocardiogram-based machine learning in long QT syndrome: a systematic review and meta-analysis.
Min-Juan Wu et al. Front Cardiovasc Med 2023 101172451
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Importance of GWAS risk loci and clinical data in predicting asthma using machine-learning approaches.
Zan-Mei Qin et al. Comb Chem High Throughput Screen 2023
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Using machine learning to develop a clinical prediction model for SSRI-associated bleeding: a feasibility study.
Jatin Goyal et al. BMC Med Inform Decis Mak 2023 23(1) 105
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 07, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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